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N/A N=75 Randomized Quadruple-blind Other

NAD+ and Exercise in FA

Friedreich Ataxia 1

Enrolled (actual)
75
Serious AEs
0.0%
Results posted
Mar 2026
Primary outcome: Primary: Within-Participant Change in Peak V02 (Maximal Oxygen Uptake on Cardiopulmonary Exercise Testing) — 0.06; -0.06; 0.1; 0.03 L/min

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Nicotinamide Riboside (Dietary_supplement); Placebo (Dietary_supplement); Exercise Intervention (Other)
Age
Pediatric, Adult · 10+ yrs
Sex
All
Sponsor
Children's Hospital of Philadelphia
Primary completion
Feb 2025

Outcome Measures

OutcomeResultp-value
PRIMARY
Within-Participant Change in Peak V02 (Maximal Oxygen Uptake on Cardiopulmonary Exercise Testing)
0.06; -0.06; 0.1; 0.03
SECONDARY
Within-Participant Change in Whole Body Insulin Sensitivity (Si)
-0.23; -0.11; -0.31; -0.51

Summary

Randomized, placebo-controlled trial with a 2x2 factorial design testing the effects of an NAD+ precursor (NR) and exercise on Peak VO2 and Si in Friedreich's Ataxia (FA). The primary objective of this research is to measure the effect of combination administration (NR + exercise) on aerobic capacity (Peak VO2) in FA. A key secondary objective is to measure the effect of combination administration (NR + exercise) on glucose homeostasis (Si) in FA.

Eligibility Criteria

Inclusion Criteria

  • Molecular diagnosis of Friedrich's Ataxia (FA).
  • Males and Females, Age 10 to 40 years (inclusive).
  • Girls, 11 years of age and older, must have a negative urine/serum pregnancy test and must use an acceptable method of contraception, including abstinence, a barrier method (diaphragm or condom), Depo-Provera, or an oral contraceptive, for the duration of the study.
  • Not currently meeting exercise guidelines as outlined by The Physical Activity Guidelines for Americans.
  • Children and Adolescents should do 60 minutes (1 hour) or more of moderate-to-vigorous physical activity daily.
  • As a part of their physical activity, children and adolescents should include muscle-strengthening physical activity on at least 3 days a week.
  • Adults should do at least 150 minutes (2 hours and 30 minutes) to 300 minutes (5 hours) a week of moderate-intensity, or 75 minutes (1 hour and 15 minutes) to 150 minutes (2 hours and 30 minutes) a week of vigorous-intensity aerobic physical activity.
  • Adults should also do muscle-strengthening activities of moderate or greater intensity that involve all major muscle groups on 2 or more days a week.
  • Cardiac echocardiogram or cardiac MRI, performed within 1 year of enrollment, showing an LVEF > 45%
  • ECG, performed within 1 year of enrollment, without clinically significant arrhythmia.
  • Weight > 24 kg
  • Parental/guardian permission (informed consent) and if appropriate, child assent.

Exclusion Criteria

  • Known sensitivity to NR.
  • Concurrent use of any medications, including statins, likely to increase risk of NR toxicity.
  • HgbA1c > 8.5% and/or Diabetes Mellitus (DM) requiring insulin or insulin secretagogue.
  • Use of supraphysiologic steroids.
  • Laboratory abnormalities that indicate clinically significant anemia or bleeding risk. (Hemoglobin < 10 g/dL or Platelets < 100K)
  • Laboratory abnormalities that indicate clinically significant kidney disease using serum creatinine and Modification of Diet in Renal Disease (MDRD) equation. (Estimated Glomerular Filtration Rate (eGFR) < 60 ml/min/1.73 m2)
  • Laboratory abnormalities that indicate clinically significant liver disease. (Aspartate Aminotransferase (AST)/Serum Glutamic Oxaloacetic Transaminase (SGOT) 3.0 x Upper Limit of Normal and/or Alanine Aminotransferase (ALT)/Serum Glutamic Pyruvic Transaminase (SGPT) 3.0 x Upper Limit of Normal)
  • Uncontrolled and persistent arrhythmias that are felt to be clinically significant.
  • Known history of moderate or severe left ventricular systolic dysfunction (Left Ventricular Ejection Fraction (LVEF) < 45%)
  • Standard contraindications to exercise testing.
  • Inability to sit and pedal unassisted in a cycle ergometry chair, at a cadence of at least 55 rotations per minute (rpm) during unloaded warm up, in a cycle ergometry chair and complete a maximal Cardio Pulmonary Exercise Test (CPET)
  • Inability to sit and pedal unassisted in a recumbent tricycle.
  • Any contraindication to MRI. Including:
  • Any intra-luminal implant, filter, stent or valve replacement
  • Any type of life assist device, pump, or prosthetic
  • Any vascular clip or clamp
  • Any surgically placed clips or clamps or bands on visceral organs
  • Any intracranial implants of any type other than dental fillings
  • Any non-removable piercings, jewelry, or medicinal patch
  • Any personal history of intraocular injury or fragment in or around the orbit that cannot be cleared through radiologic examination.
  • Any personal history of bullet, shrapnel, or stabbing wounds that cannot be cleared through radiologic evaluation.
  • Inability to lie flat in the MRI scanner for 60-90 minutes.
  • participants who cannot complete the MRI will not be excluded from participation in the remainder of the study procedures if they meet those inclusion and exclusion criteria
  • Use of any investigational agent within 4 weeks of enrollment, except open-label extension phase.
  • Females: pregnant, lactating, or planning to
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04192136). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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